摘要
目的研究汉防己甲素对人肝癌多药耐药细胞株Hep-3B/ADM耐药性的逆转作用及其机制。方法通过阿霉素(ADM)浓度梯度递增诱导法,建立人肝癌多药耐药细胞株Hep-3B/ADM。MTT法检测细胞对化学疗法药物的敏感性;流式细胞仪检测细胞表面多药耐药基因表达产物P-170及分析细胞内若丹明123染剂相对荧光强度。结果汉防己甲素(0.10~1.00μmol/L)可逆转肝癌耐药细胞的耐药性;汉防己甲素明显降低细胞表面P-170的表达。结论汉防己甲素具有增强阿霉素对Hep-3B/ADM细胞的毒性作用,其作用机制与逆转多药耐药基因有关。
Objective To investigate reversal effect on Hep-3B/ADM by TTD and its mechanism. Methods An adriamyein-resistant human HCC cell line (Hep-3B/ADM) was established, through exposure to gradually increased concentration of ADM. Drug sensitivity was measured by MTF. Flow cytometry (FCM) was performed to assess the expression of P-170 and the fluorescene intensity of Rh13 in the cells. Results ITD(0.10- 1. 00 μmol/L) can reverse multidrug-resistant of Hep-3B/ADM. TTD decreased the expression of P-170 in the cells significantly. Conclusion TTD significantly enhancs ADM-induced cytotoxicity. The mechanism is mediated by inhibiting multidrug-resistant ( MDR1 ).
出处
《中国医药》
2008年第12期790-791,共2页
China Medicine
关键词
肝癌
汉防己甲素
阿霉素
多药耐药
Hepatocellular carcinoma
Tetredrine
Adriamycin
Muhidrug-resistant